FDA 510(k) Applications Submitted by TOM BENTO

FDA 510(k) Number	Submission Date	Device Name	Applicant
K171124	04/17/2017	Nihon Kohden Wireless Input Unit WEE-1200	Nihon Kohden Corporation
K151080	04/22/2015	Nihon Kohden CSM 1901 Bedside Monitor	Nihon Kohden
K152305	08/14/2015	Nihon Kohden Afib Detection Program QP-039P	NIHON KOHDEN CORPORATION
K163459	12/09/2016	Nihon Kohden Vital Sign Telemeter	Nihon Kohden Corporation
K183529	12/19/2018	AE-120A EEG Head Set	Nihon Kohden Corporation
K153707	12/23/2015	Nihon Kohden Vital Sign Telemeter	NIHON KOHDEN CORPORATION
K163644	12/23/2016	Nihon Kohden QP-160AK EEG Trend Program	Nihon Kohden Corporation